Canonical Allele Identifier: PA2573091272
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1341357
ClinVar RCV Id: RCV001829275

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Leu389del
CA2573053118
NM_015046.7:c.1165_1167del